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SureStep™ Foley Tray System Lubri-Sil® IC Complete Care® A900414ARecalls & reported problems

C. R. Bard, Inc. · SureStep® Foley Tray System Lubri-Sil® IC Complete Care® Catheter Tray & 2000 ml Drainage Bag · Class 2

All models of SureStep Foley Tray System Lubri-Sil IC Complete Care (14)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00801741096617), received between Oct 11, 2017 and Oct 11, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Component Missing” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Component Missing1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionOct 11, 2017Component Missing

    IT WAS REPORTED THAT UPON OPENING THE FOLEY TRAY, THE CATHETER WAS MISSING.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 6942045 ↗

Other CATHETER, UROLOGICAL (ANTIMICROBIAL) AND ACCESSORIES devices

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Sources and updates

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